{{Rsnum
|rsid=386834132
|Chromosome=8
|Orientation=plus
|geno1=(-;-)
|geno2=(-;CT)
|geno3=(CT;CT)
|Gene=CLN8
|position=1780268
|Gene_s=CLN8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=8
|CLNACC=RCV000050126.1
|CLNALLE=1
|CLNDBN=Ceroid lipofuscinosis neuronal 8
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:Orphanet
|CLNDSDBID=NBK1428:C1838570:600143:168491:228354:79264
|CLNHGVS=NC_000008.10:g.1728434_1728435delCT
|CLNSIG=4
|Disease=Ceroid lipofuscinosis neuronal 8
|FwdREF=CT
|REF=TCT
|RSPOS=1728431
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386834132
|GENEINFO=CLN8:2055
|GENE_ID=2055
|GENE_NAME=CLN8
}}{{PMID Auto
|PMID=22220808
|Title=Variant late-infantile neuronal ceroid lipofuscinosis due to a novel heterozygous CLN8 mutation and de novo 8p23.3 deletion.
}}